RapidAI earns FDA clearance for PE triage software

By AuntMinnie.com staff writers

May 24, 2022 -- Artificial intelligence (AI) software developer RapidAI has secured U.S. Food and Drug Administration (FDA) 510(k) clearance for its Rapid PE Triage & Notification software platform.

Rapid PE Triage & Notification is designed to identify suspected cases of central pulmonary embolism (PE) on CT pulmonary angiography exams and provide real-time notifications to physicians, according to the vendor.

Copyright © 2022 AuntMinnie.com

To read this and get access to all of the exclusive content on AuntMinnie.com create a free account or sign-in now.

Member Sign In:
MemberID or Email Address:  
Do you have a AuntMinnie.com password?
No, I want a free membership.
Yes, I have a password:  
Forgot your password?
Sign in using your social networking account:
Sign in using your social networking